2,8,9-Triisopropyl-2,5,8,9-tetraaza-1-phosphabicyclo[3,3,3]undecane

Base Information

• Chemical Name: 2,8,9-Triisopropyl-2,5,8,9-tetraaza-1-phosphabicyclo[3,3,3]undecane
• CAS No.: 175845-21-3
• Molecular Formula: C₁₅H₃₃N₄P
• Molecular Weight: 300.428
• DSSTox Substance ID: DTXSID70408791
• Nikkaji Number: J770.622G
• Wikidata: Q72515260
• Mol file: 175845-21-3.mol

Synonyms:175845-21-3;2,8,9-Triisopropyl-2,5,8,9-tetraaza-1-phosphabicyclo[3,3,3]undecane;2,8,9-Tri-I-Propyl-2,5,8,9-Tetraaza-1-Phosphabicyclo[3.3.3]Undecane;2,8,9-tri(propan-2-yl)-2,5,8,9-tetraza-1-phosphabicyclo[3.3.3]undecane;2,8,9-TRIISOPROPYL-2,5,8,9-TETRAAZA-1-PHOSPHABICYCLO[3.3.3]UNDECANE;[2,5,8,9-Tetraaza-1-phosphabicyclo[3.3.3]undecane-2,8,9-tris(1-methylethyl)];2,5,8,9-Tetraaza-1-phosphabicyclo[3.3.3]undecane, 2,8,9-tris(1-methylethyl)-;DFRWCJYSXGNOFD-UHFFFAOYSA-N;SCHEMBL244329;DTXSID70408791;BCP27441;2,8,9-Triisopropyl-2,5,8,9-tetraza-1-phosphabicyclo[3.3.3]undecane;MFCD03701530;AKOS015912888;CS-0108401;A15305;J-011138;2,8,9-triisopropyl-2,5,8,9-tetraaza-1-phospha-bicyclo[3.3.3]undecane

Chemical Property of 2,8,9-Triisopropyl-2,5,8,9-tetraaza-1-phosphabicyclo[3,3,3]undecane

Chemical Property:

• Vapor Pressure: 4.12E-05mmHg at 25°C
• Refractive Index: n20/D 1.4830(lit.)
• Boiling Point: 351.4°C at 760 mmHg
• Flash Point: 46 °F
• PSA: 26.55000
• Density: 0.922 g/mL at 25 °C(lit.)
• LogP: 2.42530
• Sensitive.: moisture sensitive
• XLogP3: 2.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 300.24428407
• Heavy Atom Count: 20
• Complexity: 261

Purity/Quality:

97% ^*data from raw suppliers

2,8,9-Tri-i-propyl-2,5,8,9-tetraaza-1-phosphabicyclo[3.3.3]undecane ^*data from reagent suppliers

Safty Information:

• Hazard Codes: F,Xn
• Statements: 11-38-48/20-63-65-67
• Safety Statements: 36/37-62-24/25-16

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC(C)N1CCN2CCN(P1N(CC2)C(C)C)C(C)C
• Uses: Base used in an attempt to produce higherly reactive no-carrier-added fluoride for labeling of radiopharmaceuticals and used in the synthesis of monomeric alumatranesDeprotonation agent used to study the nucleophilic reactivities of benzenesulfonyl-substituted carbanionsCatalyst involved in: Synthesis of polymer-supported proazaphosphatranes for catalysis of amidation and transesterification reactionsWadsworth-Emmons reactionsMukaiyama aldol reactionsSynthesis of aryl alcohols via addition reactions